CBD reshapes prostate cancer cells and boosts drug effects

Cannabidiol alters the epigenome of hormone-dependent prostate cancer cells.

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie β€’ β€’ Highly Relevant
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AI Summary

This laboratory study examined whether cannabidiol (CBD) affects hormone-dependent prostate cancer cells through changes in gene activity and the epigenomeβ€”chemical modifications that help control which genes are switched on or off. Across several prostate cancer cell models, CBD changed methylation patterns and influenced the expression of epigenetic regulators including DNMT1 and EZH2, although EZH2’s catalytic activity did not change.

CBD also produced widespread changes in gene expression, especially in LNCaP cells, including disruption of cell-cycle pathways and reduced activity of key regulators such as CDK1 and CDK2. It lowered cancer-cell viability in a dose-dependent manner and showed additive or synergistic effects when combined with targeted or hormonal treatments. These results suggest CBD may have potential as an add-on cancer therapy, but they come from cell-line experiments and do not show that CBD treats prostate cancer in people or establish a safe or effective dose for cannabis users.

πŸ’‘ Key Findings

1
CBD altered the epigenome of prostate cancer cells, including methylation patterns in LNCaP cells and expression of the regulators DNMT1 and EZH2.
Limited
35%
2
CBD caused widespread gene-expression changes, particularly in LNCaP cells, with effects on cell-cycle regulation and reduced expression of CDK1 and CDK2.
Limited
35%
3
CBD reduced prostate cancer cell viability in a dose-dependent manner in laboratory models.
Limited
35%
4
CBD showed additive or synergistic effects when combined with targeted and hormonal cancer therapies in these cell experiments.
Limited
35%

πŸ“„ Original Abstract

Cannabidiol (CBD) shows promising anti-cancer effects, including reducing proliferation and migration and inducing cell death. However, its impact on cancer gene regulation and epigenetic mechanisms remains poorly understood, particularly in prostate cancer, a disease characterised by widespread epigenetic alterations. This study investigated whether CBD exerts anti-cancer effects in prostate cancer by modulating cell viability, gene expression, and the epigenome and whether it enhances the efficacy of targeted and hormonal agents. Prostate cancer cell lines (DU145, PC3, LNCaP) were treated with varying concentrations of CBD, Talazoparib, GSK126 and enzalutamide. Cell viability was assessed by MTT. Transcriptomic changes were analysed by RNAseq and qRT-PCR, and epigenetic effects were evaluated by the Infinium MethylationEpic V2.0 BeadChip array. Analysis of total 5mC and expression/activity of EZH2 were assessed by ELIZA and Western blot respectively. Epigenetically, CBD altered methylation patterns in LNCaP cells, while modulating DNMT1 and EZH2 expression across models. However, EZH2 catalytic activity was unchanged. CBD induced widespread transcriptional changes, particularly in LNCaP cells, with enrichment of cell cycle pathways and downregulation of key regulators (e.g., CDK1/2). CBD reduced cell viability in a dose-dependent manner, showing additive or synergistic effects with both targeted and hormonal therapies. CBD exerts anti-cancer effects in prostate cancer, potentially through disruption of cell cycle regulation and epigenetic modulation. These findings support its potential as a therapeutic agent, particularly in combination with targeted treatments.

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